1jpf
From Proteopedia
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Crystal Structure Of The LCMV Peptidic Epitope Gp276 In Complex With The Murine Class I Mhc Molecule H-2Db
Overview
Class I major histocompatibility complex (MHC) molecules, which display, intracellularly processed peptides on the cell surface for scanning by, T-cell receptors (TCRs), are extraordinarily polymorphic. MHC polymorphism, is believed to result from natural selection, since individuals, heterozygous at the corresponding loci can cope with a larger number of, pathogens. Here, we present the crystal structures of the murine MHC, molecule H-2D(b) in complex with the peptides gp276 and np396 from the, lymphocytic choriomeningitis virus (LCMV), solved at 2.18 A and 2.20 A, resolution, respectively. The most prominent feature of H-2D(b) is a, hydrophobic ridge that cuts across its antigen-binding site, which is, conserved in the L(d)-like family of class I MHC molecules. The comparison, with previously solved crystal structures of peptide/H-2D(b) complexes, shows that the hydrophobic ridge focuses the conformational variability of, the bound peptides in a "hot-spot", which could allow optimal TCR, interaction and discrimination. This finding suggests a functional reason, for the conservation of this structural element.
About this Structure
1JPF is a Protein complex structure of sequences from Mus musculus. Full crystallographic information is available from OCA.
Reference
Zooming in on the hydrophobic ridge of H-2D(b): implications for the conformational variability of bound peptides., Ciatto C, Tissot AC, Tschopp M, Capitani G, Pecorari F, Pluckthun A, Grutter MG, J Mol Biol. 2001 Oct 5;312(5):1059-71. PMID:11580250
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